Imatinib is an oral cancer medicine that blocks several tyrosine kinase enzymes, including the abnormal BCR-ABL protein produced by the Philadelphia chromosome. By locking this enzyme in an inactive shape, it slows the growth of cancer cells and can trigger their death. It treats chronic myelogenous leukemia, Philadelphia chromosome positive acute lymphocytic leukemia, gastrointestinal stromal tumors, and several rarer blood and skin cancers. Scientists at Ciba-Geigy, later Novartis, developed the compound in the early 1990s under the direction of Nicholas Lydon, and oncologist Brian Druker of Oregon Health and Science University led its clinical testing. The United States Food and Drug Administration approved it in May 2001, only about two and a half years after the new drug application was filed, an unusually fast review credited to its striking early trial results.
Facts
Classification
Approval Status ATC ClassSourced to the subject's own accountL: Antineoplastic and Immunomodulating Agents 2 Route of Administration WHO Essential MedicineSourced to the subject's own account First Approved / Isolated Year Connections
Sources
1. Imatinib (Wikipedia)
2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code LQuote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
View the Source 3. Imatinib (Wikipedia)
WikipediaInfobox drug, routes_of_administrationQuote, Infobox drug, routes_of_administration
By mouth
View the Source 4. WHO Model List of Essential Medicines (Wikipedia)
WikipediaWHO Model List of Essential Medicines, Targeted therapies sectionQuote, WHO Model List of Essential Medicines, Targeted therapies section
Imatinib
View the Source 5. Drugs.com: Gleevec (imatinib mesylate) FDA Approval History
FDA Approval HistoryQuote, FDA Approval History
Gleevec (imatinib mesylate) was first approved by the FDA on May 10, 2001
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